EP4330678A1 - Auf mikrokompartment basierendes interaktionsscreening mit hoher komplexität - Google Patents
Auf mikrokompartment basierendes interaktionsscreening mit hoher komplexitätInfo
- Publication number
- EP4330678A1 EP4330678A1 EP22721802.1A EP22721802A EP4330678A1 EP 4330678 A1 EP4330678 A1 EP 4330678A1 EP 22721802 A EP22721802 A EP 22721802A EP 4330678 A1 EP4330678 A1 EP 4330678A1
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- European Patent Office
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Classifications
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/68—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving proteins, peptides or amino acids
- G01N33/6803—General methods of protein analysis not limited to specific proteins or families of proteins
- G01N33/6845—Methods of identifying protein-protein interactions in protein mixtures
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
- C12N15/1034—Isolating an individual clone by screening libraries
- C12N15/1037—Screening libraries presented on the surface of microorganisms, e.g. phage display, E. coli display
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N15/00—Mutation or genetic engineering; DNA or RNA concerning genetic engineering, vectors, e.g. plasmids, or their isolation, preparation or purification; Use of hosts therefor
- C12N15/09—Recombinant DNA-technology
- C12N15/10—Processes for the isolation, preparation or purification of DNA or RNA
- C12N15/1034—Isolating an individual clone by screening libraries
- C12N15/1075—Isolating an individual clone by screening libraries by coupling phenotype to genotype, not provided for in other groups of this subclass
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/68—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions involving nucleic acids
- C12Q1/6813—Hybridisation assays
- C12Q1/6816—Hybridisation assays characterised by the detection means
- C12Q1/6818—Hybridisation assays characterised by the detection means involving interaction of two or more labels, e.g. resonant energy transfer
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2319/00—Fusion polypeptide
- C07K2319/20—Fusion polypeptide containing a tag with affinity for a non-protein ligand
- C07K2319/21—Fusion polypeptide containing a tag with affinity for a non-protein ligand containing a His-tag
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- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07K—PEPTIDES
- C07K2319/00—Fusion polypeptide
- C07K2319/40—Fusion polypeptide containing a tag for immunodetection, or an epitope for immunisation
- C07K2319/42—Fusion polypeptide containing a tag for immunodetection, or an epitope for immunisation containing a HA(hemagglutinin)-tag
Definitions
- the invention regards a method for screening for interactions between two compounds provided in libraries.
- the invention in particular provides a method for screening interactions, such as a binding between two molecules or macromolecules, that is not limited to a classical screening by bait and prey setup, and therefore allows for a high-complexity screening of large candidate libraries, including screening for immunological interactions such as interactions between T-cells and antigen presenting cells, or B-cells and their antigenic targets.
- DESCRIPTION Cell-signalling is governed by different interactions between binding partners. These interactions lead to the attainment of a function or communication between at least two entities.
- the method describes a highly complexed approach for screening binding interactions of natural (e.g. proteins, antibodies) or synthetic (e.g. drugs) partners.
- natural e.g. proteins, antibodies
- synthetic e.g. drugs
- many different technologies have been established to screen highly complex libraries of biomolecules (such as antibodies, proteins, peptides or nucleic acids) or synthetic organic molecules in order to identify new therapeutics.
- DEL DNA-encoding libraries
- HTS high throughput screening
- Identifying binding interactions is an important task in biological and medical sciences. Interactions of proteins, nucleic acids with each other or chemical compounds or metabolites provide important clues about cellular signalling networks and metabolic and genetic regulation mechanisms. Moreover, inhibitors of such interactions are important pharmaceuticals, so there is a direct impact of the elucidation of biological interactions on medicine. Screening methods can be separated essentially into two groups: in the first group, interacting targets are identified as such, i.e. the identification method comprises a step wherein the information comprised in the protein or other molecule itself is used for identification. Examples for methods falling into this group are immunoprecipitation, surface plasmon resonance screening, or peptide-array screening methods. Identification of proteins is accomplished e.g. by sequence determination through Edman-degradation or mass-spectrometiy of peptides derived from the protein.
- the protein and the sequence coding for it are coupled tightly, e.g. by maintaining both in close spatial proximity.
- assays exemplified by phage display (Bratkovic T. (2010) “Progress in phage display: evolution of the technique and its application” Cell Mol Life Sci. Mar;67(5):749-707) or the various types of two-hybrid screening methods (Dove and Hochschild (2004), "A bacterial two-hybrid system based on transcription activation", Methods Mol Biol. 261:231-4; Briickner et al. (2009), 'Yeast two-hybrid, a powerful tool for systems biology", Int J Mol Sci.
- Known droplet-based microfluidic applications as shown for example in WO 2016/048994 are used with in vitro two-hybrid system (IVT2H) and one library to identify potential peptide binder.
- IVT2H in vitro two-hybrid system
- the droplets are generated using an initial microfluidic device to encapsulate one gene per droplet. After an incubation time, the droplets that contain a protein interaction will lead to the production of a fluorescent signal (e.g. GFP) and will be detected and sorted accordingly using a second microfluidic device.
- a fluorescent signal e.g. GFP
- the microfluidic workflow is more complex and requires a consequent installation and know-how with the use of lasers and sorting.
- Thermal proteome profiling (Mateus et al. 2020, Molecular Systems Biology, 16(3), 1-11.) is a mass spectrometry based proteomic analysis method that can be used to identify protein interactions with small molecules, metabolites or other proteins. This method is based on the effect that proteins change their thermostability behaviour upon interacting with another molecule. The current biggest limitation of this approach is its low throughput due to the nature of mass spectrometry-based proteomics.
- screening assays of the second group are usually performed keeping one interaction partner constant (the “bait” protein), whereas the other interaction partner normally is provided as a library of candidate proteins (the “prey” proteins) that are expressed within a test- cell.
- Prey proteins interacting with the bait are identified by sequencing the nucleic acid sequences encoding the said prey proteins within a biological cell. Efficiency of such assays is limited since single clones have to be isolated to make sequencing possible. So, it is desirable to develop protein-protein interaction screening methods allowing for a more efficient screening and in particular a screening in higher complexity with respect of number of screened candidate interaction pairs.
- the invention pertains a method for the identification of at least two interacting entities comprised in two separated libraries of candidate interacting entities, the method comprising the steps of:
- step (d) Detecting subsequent to step (c) within the plurality of compartments, which comprise encapsulated entities, a presence of, and preferably an identity of, at least two labelling-portions encapsulated within a single compartment, wherein the presence of two labelling portions within a single compartment is indicative for an interaction between the two candidate interacting entities encapsulated within said compartment.
- the invention pertains to a method for screening for interaction between two entities each of which are comprised in a plurality of entities (library), the method comprising performing the steps of the method of the first aspect.
- the invention solves the indicated problem in a first aspect by a method for the identification of at least two interacting entities comprised in two separated libraries of candidate interacting entities, the method comprising the steps of:
- a ratio of entities to compartments which is larger than o and less than 1 (preferably less than 0.1);
- step (d) Detecting subsequent to step (c) within the plurality of compartments, which comprise encapsulated entities, a presence of, and preferably an identity of, at least two labelling-portions encapsulated within a single compartment, wherein the presence of two labelling portions within a single compartment is indicative for an interaction between the two candidate interacting entities encapsulated within said compartment.
- the present invention seeks to identify interacting entities based on the idea that if an interaction complex of two interacting entities (molecules) is formed, such complex can be separated from non-interacting entities in close spatial proximity by encapsulation of the complex at very low entity concentration. The reduction of the concentration results in an encapsulation of on average less than one entity or interacting complex.
- non-interacting entities e.g. phage particles displaying proteins that do not bind to any other within the library to be tested
- entities interacting with each other e.g. a phage particle displaying a protein drug target and another one displaying an antibody binding to it
- fusion PCR also known as overlap extension PCR
- a forward primer binding to the backbone encoding all members of library one e.g. the antibody library
- a reverse primer binding to the backbone encoding all members of library two e.g. open reading frames of all proteins of a pathogen as potential drug targets.
- an identification of the interacting entities can be performed in an additional step. While the present invention is exemplified using nucleic acid-based hybridization and amplification techniques for the final step of determining entity identity, the invention shall not necessarily be restricted to nucleic acid-based methods.
- Primer selection for such fusion PCR allows for the generation of a PCR product that combines the sequences of the labelling portions of both libraries.
- the labelling portion of each entity comprises a sequence that is specific to the individual entity, and a further (outer) sequence specific for the library the entity is contained in. This allows a use of two separate primer pairs of which each amplify only a labelling portions of an entity of one library.
- at least one of each primer of each set comprises an overlapping section complementaiy with an overlapping section of one primer used for the amplification in the other library. Therefore, during PCR a larger PCR product can be generated (see figure 1).
- a set of primers that comprise a hybridization element specific for each library identifying sequence. Such overlapping primer section can be introduced into either the “inner” or “outer” primers.
- the candidate entity of one or more candidate entity libraries of the invention is a cell.
- the invention seeks to screen for interactions between cells and another entity or between cells.
- Such cell-based interactions including cell-to-cell interactions are based on cell-surface based interaction components, such as receptor-ligand interactions, which mediate very specific cell mediated interactions.
- cell-based screens including cell-to-cell interaction screens, in immunology, for example for the development of T-cell based therapeutics.
- the invention comprises an interaction screen for the identification of matching pairs of T-cell receptors (TCRs, displayed on T-cells) and antigens (peptide antigens displayed on the MHC2 complex of antigen presenting cells, APCs).
- TCRs T-cell receptors
- antigens peptide antigens displayed on the MHC2 complex of antigen presenting cells, APCs.
- the invention therefore pertains to a method as described herein before, wherein the candidate entity libraries are cell libraries comprising a plurality of cells presenting a variety of different MHC bound peptides on the one hand, and a second candidate entity library comprising cells each expressing a particular T-cell receptor clone.
- the antigenic peptide is loaded on to the APC.
- the term “antigen presenting cell” includes a B cell, dendritic cell, macrophage, activated epithelial cell, fibroblast, thymic epithelial cell, thyroid epithelial cell, glial cell, pancreatic beta cell, and a vascular endothelial cell.
- the APC is a professional APC such as a dendritic cell, macrophage, B cell, or an activated epithelial cell.
- the APC is a non-professional APC such as a fibroblast, thymic epithelial cell, thyroid epithelial cell, glial cell, pancreatic beta cell, or a vascular endothelial cell. Since cancer cells also act as antigen presenting cells, the term "antigen presenting cell" further includes cancer cells.
- MHC may include both MHC or HLA class I and MHC or HLA class II complexes.
- the invention pertains both to CD4 and CD8 positive T cells, depending on the specific interaction to be screened.
- the present invention surprisingly provides a further screening method for the identification of a specific immunological cell-to-cell interactions, such as an interaction between a T-cell receptor and an MHC-presented antigenic peptide.
- the surprising aspect of the invention lies in the fact that the interaction between TCR expressing T-cells and antigen presenting cells (APCs) is detectable as duplet formation (or two-entity complexes), and therefore can be subjected to the screening method of the invention comprising compartmentalization of the cell duplets.
- the invention can be used to detect an interaction between B- cell receptor expressing B-cells and a target antigen (and/or cell surface expressed antigen).
- the first candidate entity library is a library of T-cell, wherein each T-cell comprises one distinct and rearranged T-cell receptor gene encoding for a specific T-cell receptor.
- the second candidate entity library is a library of antigen presenting cells, wherein each antigen presenting cell comprises on its surface an MHC complex presenting an antigenic peptide with a specific sequence.
- one of the candidate entity libraries is a B-cell library expressing one distinct and rearranged B-cell receptor gene encoding for a specific B-cell receptor.
- the second library can be selected from a library of candidate soluble antigens, or cells expressing cell surface located candidate antigens.
- the labelling portion which is a nucleic acid may comprise a hybridization portion that is specific for a certain library of entities.
- Such hybridization portions in this embodiment preferably comprise a sequence which is complementary to, or hybridizes under stringent conditions to, a second hybridization portion comprised in a labelling portion of entities of a second, and different library.
- screening approaches an interaction of the entities of both libraries to one another may be screened. If interacting entities are encapsulated, the hybridization portions of both candidate interacting entities can hybridize and form a fused template for a fusion PCR.
- the labelling portions which are nucleic acids may be simply ligated together, either blunt or using short overhangs.
- the primer which is not used for linking (overlap) may in addition comprise an outer hybridization element that can be used for a second PCR in order to exponentially amplify the fused PCR product.
- fusion PCR or “overlap extension PCR” means that the PCR products are formed into overlapping chains by using primers having complementary ends, thereby overlapping the amplified fragments of different sources by overlapping extension chains in subsequent amplification reactions.
- the amplification reaction is performed with a higher concentration of outer primers compared to the inner primer pair (such as preferably 2 fold, 3 fold, 4 fold, 6 fold, 8 fold or 10 fold, too fold or higher). This embodiment allows for a stronger amplification of the fused product compared to possible shorter non interaction dependent amplification products.
- a ratio of entities to compartments in step (c) is in certain embodiments larger than o and less than 1, preferably which is larger than o and in increasing preference less than 0.5, 0.2, 0.1, 0.05, most preferably less than 0.01.
- An “interacting entity” in context of the invention shall be any molecule or molecule complex, which can form a non-covalent or covalent interaction with another interacting entity.
- the interacting entities form specific and selective interactions with each other.
- a typical example of interacting entity pairs in accordance with the present invention are interaction pairs such as antibody-antigen, nucleic acid hybridization, receptor-ligand, enzyme-substrate, small molecule inhibitor and target protein, etc.
- An entity libraiy in accordance with the present invention comprises a plurality of distinct single entities.
- the entity library can have from 10 to to 9 candidate entity members, e.g., from 10 candidate entities to 10 2 candidate entities, from 10 2 candidate entities to 10 3 candidate entities, from io 3 candidate entities to io 4 candidate entities, from io 4 candidate entities to io 5 candidate entities, from io 5 candidate entities to io 6 candidate entities, from io 6 candidate entities to io 7 candidate entities, from io 7 candidate entities to io 8 candidate entities, or from io 8 candidate entities to to 9 candidate entities.
- the library has more than io 9 candidate entities.
- the method of the invention comprises a purification step between steps (b) and (c) in order to remove non interacting entities which are not in an interaction complex.
- the candidate interacting entities of the libraries further comprise purification tags which are representative for their libraiy. Including a step of purification using the purification tag of a given entity libraiy, entities of the other libraries which are not within an interaction-complex will be discriminated against in the purification, and their fraction is accordingly reduced.
- the method may therefore comprise a purification step for each species of entity library used in the method. Such multiple purification steps are done in sequence and preferably not concomitantly.
- the ratio of entities to compartments in step (c) is preferably 0,1 or larger, and less than 1; more preferably is larger than 0.1 and less than 1, for example is about 0.5.
- a preferred entity library of the invention is a library of molecules attached to a nucleic acid labelling portions, also known as DNA-encoded library technology (DELT).
- a DNA-encoded library (DEL) is composed of a pool of different molecules, each being a conjugate between a small organic molecule and a specific DNA sequence (a so-called "DNA barcode" which shall be understood to constitute a labelling portions in context of the present invention), thus realizing a direct physical connection between function, such as function of the candidate entity molecule by its chemical structure as an interacting entity) and information (information about the type of small organic molecule coded by the DNA sequence).
- the DNA sequences are designed to identify the associated chemical structures of the candidate entity using various technologies, e.g.
- Candidate entities used in DELs may range from small or large organic molecules to biomolecules such as proteins, sugars, nucleic acids, fatty acids, or any combination of the forgoing.
- the method of the present invention is performed extra cellular, in other words, the screening steps (a) to (d) are performed without performing a protein expression and/or presentation within a biological cell.
- binding refers to a direct association between two entities such as molecules (e.g., two polypeptides of a protein-protein interaction pair), due to, for example, covalent, electrostatic, hydrophobic, and ionic and/or hydrogen-bond interactions, including interactions such as salt bridges and water bridges.
- a “specific binding” refers to binding with an affinity between two protein interaction entities of at least about to -7 M or greater, e.g., 5x1o 7 M, to -8 M, 5x1o 8 M, and greater.
- non-specific binding refers to binding with an affinity of less than about to -7 M, e.g., binding with an affinity of to -6 M, to -5 M, to -4 M, etc.
- “specific binding” can be lower than 10 7 M; e.g., specific binding can be binding with an affinity of at least to -5 M or greater, e.g., to -5 M, to -6 M, or to -7 M. Binding affinities can depend on the chemical environment, e.g. the pH value, the ionic strength, the presence of co-factors, etc.
- protein-protein interaction can refer to protein-protein interactions occurring under physiological conditions, i.e. under conditions found in a living cell.
- polypeptide refers to a polymeric form of amino acids of any length, which can include genetically coded and non- genetically coded amino acids, chemically or biochemically modified or derivatized amino acids, and polypeptides having modified peptide backbones.
- the term includes fusion proteins, including, but not limited to, fusion proteins with a heterologous amino acid sequence, fusions with heterologous and homologous leader sequences, with or without N-terminal methionine residues; immunologically tagged proteins; and the like.
- the first and the second members of the first candidate entity library and a second candidate entity library are naturally-occurring polypeptides.
- one or both of the first and the second members of the candidate libraries is a non-naturally-occurring polypeptide, e.g., a recombinant polypeptide made in the laboratory, or mutated compared to a naturally-occurring polypeptide.
- the first member of the protein interaction pair is an N-terminal portion of a polypeptide; and the second member of the protein interaction pair is a C-terminal portion of the polypeptide.
- the first member of the protein interaction pair is a known protein; and the second member of the protein interaction pair is an unknown protein, e.g., a member of a library of proteins.
- the first member of the protein interaction pair is a first known protein that binds to a second known protein, and the second member of the protein interaction pair is a variant of the second known protein.
- the first or second candidate entity library may comprise a limited number of members, even only one known candidate interacting entity.
- the first member of an interaction pair to be screened (which first member maybe referred to as a “bait”) is a small selection of known polypeptides; and the second member of the interaction pair (which second member maybe referred to as a “prey”) is a member of a library of proteins (e.g., a plurality of proteins) of unknown amino acid sequence and/or function.
- the known interaction partner can be any of a variety of selection of molecules, for example for proteins they may include membrane proteins, receptors, enzymes, cytoskeletal proteins, regulatory proteins, transcription factors, and the like.
- the unknown protein can be a member of a candidate compound library, where the compound library can have from 10 to to 9 members, e.g., from io members to io 2 members, from io 2 members to io 3 members, from io 3 members to io 4 members, from io 4 members to io 5 members, from io 5 members to io 6 members, from io 6 members to io 7 members, from io 7 members to io 8 members, or from io 8 members to io 9 members.
- the library has more than io 9 members.
- the interacting-portion of the invention may be selected from any molecular entity of interest including and includes a candidate entity which may be one selected from a polypeptide, peptide, glycoprotein, a peptidomimetic, an antigen binding construct (for example, an antibody, antibody-like molecule or other antigen binding derivative, or an or antigen binding fragment thereof), a nucleic acid such as a DNA or RNA, for example an antisense or inhibitory DNA or RNA, a ribozyme, an RNA or DNA aptamer, RNAi, siRNA, shRNA and the like, including variants or derivatives thereof such as a peptide nucleic acid (PNA).
- a candidate entity which may be one selected from a polypeptide, peptide, glycoprotein, a peptidomimetic, an antigen binding construct (for example, an antibody, antibody-like molecule or other antigen binding derivative, or an or antigen binding fragment thereof), a nucleic acid such as a DNA or RNA, for example an
- the candidate entity is a small (organic) molecule of any kind.
- a small molecule is a compound having a molecular mass of less than about 750 Da, such as less than about 650 or 600 Da, (and in certain embodiments, a small molecule maybe less than about 550 or 500 Da).
- the interacting-portion is a part of a macro-molecule or molecule complex that mediates the interaction for which a screening according to the invention is performed.
- the interacting-portion is a proteinaceous molecule, or is a polypeptide or a section or domain of a polypeptide, such as a domain known to mediate an interaction to other entities.
- Such an interacting domain maybe known to mediate protein-protein interactions such as immunoglobulin domains, or can be a domain comprising an active site of enzyme and known to bind small molecular substrates etc.
- small organic or inorganic compound libraries comprising labelled small molecules, for example labelled with nucleic acids, may be used for a screening in accordance with the present invention. Mixed approaches where one library is for example a protein library and the other a library is composed of small molecules, for example potential inhibitors of a protein, are in particular encompassed by the present invention.
- the labelling portion may be any molecular entity that allows for a determination of the presence or absence of the candidate entity.
- the labelling portion allows in addition for the identification of the entity - in such case, the labelling portion may also be referred to as a “barcoding portion”, or a “barcode”.
- nucleic acid- based barcode identification and/or quantification is performed by sequencing, including e.g., Next Generation Sequencing methods, conventional considerations for barcodes detected by sequencing will be applied.
- barcodes and/or kits containing barcodes and/or barcode adapters may be used or modified for use in the methods described herein, including e.g., those barcodes and/or barcode adapter kits commercially available from suppliers such as but not limited to, e.g., New England Biolabs (Ipswich, Mass.), Illumina, Inc. (Hayward, Calif.), Life Technologies, Inc. (Grand Island, N.Y.), Bioo Scientific Corporation (Austin, Tex.), and the like, or maybe custom manufactured, e.g., as available from e.g., Integrated DNA Technologies, Inc. (Coralville, Iowa).
- suppliers such as but not limited to, e.g., New England Biolabs (Ipswich, Mass.), Illumina, Inc. (Hayward, Calif.), Life Technologies, Inc. (Grand Island, N.Y.), Bioo Scientific Corporation (Austin, Tex.), and the like, or maybe custom manufactured, e.g., as
- Barcode length will vary and will depend upon the complexity of the candidate entity library and the barcode detection method utilized.
- nucleic acid barcodes e.g., DNA barcodes
- design, synthesis and use of nucleic acid barcodes is within the skill of the ordinary relevant artisan.
- each distinct candidate interacting entity comprises a nucleic acid molecule having at least one identification- sequence which is unique to the interacting-portion of the distinct candidate interacting entity.
- sequence of the barcode codes for which interacting portion (or candidate interacting entity) and therefore, detection of the presence of a unique barcode sequence indicates the presence of and identity of a unique interacting portion.
- a “barcode sequence” in the present context preferably relates to a nucleic acid sequence allowing for an unambiguous identification of the interaction portion having said barcode sequence.
- a barcode sequence consists of a sequence of at least ten, at least eleven, at least twelve, at least thirteen, at least fourteen, at least fifteen, at least sixteen, at least eighteen, at least twenty consecutive randomly assembled nucleotides.
- said barcode sequence is theoretically unique. It is well known in the art how random sequences can be achieved in oligonucleotide synthesis.
- the number of different polynucleotide molecules theoretically possible is directly dependent on the length of the barcode sequence; e.g., if a DNA barcode with randomly assembled Adenine, Thymidine, Guanosine and Cytidine nucleotides is used, the theoretical maximal number of barcode sequences possible is 1,048,576 for a length of ten nucleotides, and is 1,073,741,824 for a length of fifteen nucleotides.
- the length of the barcode sequences is selected such that the number of unique sequences theoretically possible is at least as high as the number of preys used in a pool of sequences. The person skilled in the art knows how to adopt the length of the barcode sequence.
- said barcode sequences are inserted into a pre-defined nucleotide sequence, e. g. a restriction enzyme recognition site, such that the start point of said barcode sequence is pre-determined unambiguously.
- the identification sequence or barcode sequence comprises a nucleic acid sequence encoding at least parts of the amino acid sequence of the proteinaceous interacting-portion.
- the identification sequence is flanked by an upstream primer binding sequence and a downstream primer binding sequence, which both are different and do not anneal to each other during an annealing phase of a PCR amplification cycle.
- the method may include an amplification step in order to detect the presence and identity of a barcode sequence.
- the method of the invention may comprise that step (d) involves a PCR amplification, preferably a fusion PCR and wherein the means for identifying of one or more labelling portion comprises components sufficient for conducting the PCR amplification, preferably the fusion PCR.
- fusion PCR refers to PCR methodology which is used to join or fuse a plurality of polynucleotide fragments into a conjoined polynucleotide fragment.
- Such “means for identifying of one or more labelling portion” in preferred embodiments of the invention comprise a first and a second PCR primer pair, wherein the upstream primer of the first PCR primer pair anneals to the upstream primer binding sequence of each labelling- portion contained in the first candidate entity libraiy, and the downstream primer of the first PCR primer pair anneals to the downstream primer binding sequence of each labelling-portion contained in the first candidate entity library; and wherein the upstream primer of the second PCR primer pair anneals to the upstream primer binding sequence of each labelling-portion contained in the second candidate entity library, and the downstream primer of the second PCR primer pair anneals to the downstream primer binding sequence of each labelling-portion contained in the second candidate entity library.
- a “primer binding sequence” as used herein relates to a nucleic acid sequence known to specifically hybridize to a predefined PCR primer under conditions typically used in PCR or other polynucleic acid amplifying methods.
- the primer binding sequence of the current invention consists of at least fifteen, at least sixteen, at least seventeen, at least eighteen consecutive nucleotides with a known sequence.
- the polynucleotide of the invention comprises two primer binding sequences, wherein the melting temperature of the primer binding sequences differs by no more than six, no more than five, no more than four, no more than tree, or no more than two degrees Celsius.
- the first and the second primer binding sequence differ in their nucleotide sequence to such an extent that an oligonucleotide specifically hybridizing to the first primer binding sequence does not hybridize specifically to the second primer binding sequence and that a primer specifically hybridizing to the second primer binding sequence does not hybridize specifically to the first primer binding sequence.
- the term “flanked” means being arranged in close proximity.
- the barcode sequence of the current invention is flanked by a first and a second primer binding sequence such that a nucleic acid produced by PCR using primers hybridizing specifically to said first and second primer binding sequences will consist of no more than 300, no more than 250, no more than 200, no more than 150, no more than too, no more than 75, or no more than 50 nucleotides. More preferably, the first and the second primer binding sequence are separated from the barcode sequence by no more than ten, eight, six, five, four, three, or two nucleotides. [45] In some embodiments of the invention, each primer binding sequence of the labelling portion of the candidate interacting entity of the first candidate entity library differs from each primer binding sequence of the labelling portion of the candidate interacting entity of the second candidate entity library (and vice versa).
- the upstream- and the downstream primer of the first primer pair comprises a first cross-hybridization sequence and the upstream- and the downstream primer of the second primer pair comprises a second cross-hybridization sequence; wherein the first- and the second cross-hybridization sequence hybridize to each other under annealing conditions during a PCR annealing step.
- a PCR amplification in step (c) may comprise a fusion PCR immediately followed by the removal of residual primer oligonucleotides and the subsequent nested PCR using (i) an upstream primer which anneals to the upstream primer binding sequence of each labelling-portion contained in the first candidate entity library, and a downstream primer which anneals to the downstream primer binding sequence of each labelling-portion contained in the second candidate entity library; or (ii) an upstream primer which anneals to the upstream primer binding sequence of each labelling-portion contained in the second candidate entity library, and a downstream primer which anneals to the downstream primer binding sequence of each labelling-portion contained in the first candidate entity library; wherein step (d) involves the detection of the amplification product of the nested PCR and wherein the presence of an amplification product indicates the presence of two labelling portions within a single compartment.
- the amplification product so produced allows therefore the detection of the interaction, and, if sequenced, in some embodiments also the identification of the interacting entities.
- the method of the invention may further comprise a step of sequencing the amplification product of the nested PCR in order to determine the identity of the interacting-portions which were comprised within one compartment.
- the invention in some embodiments, may also be realized using an indirect labelling of individual entities in one or more candidate entity libraries.
- the invention pertain to candidate entities wherein the labelling portion is a binding portion, such as an amino acid epitope, which allows for a specific binding of a labelling entity to the candidate entity.
- the labelling entity comprises a binding portion mediating the binding to the candidate entity, and a labelling portion, such as a nucleic acid-based label or barcode, which then allows for a detection of an interaction of two or more candidate entities.
- a binding interaction between a candidate entity and a labelling entity may be based on any specific and/or selective protein-protein or protein-nucleic acid interactions known in the art, but preferably include protein epitope tag based technologies selected from the list of interaction partners including but not limited to: antibodies, and any derivatives, variants or fragments thereof, such as nanobodies, or single-chain fragments (scFv, or scFab), nucleic acid aptamers, and similar proteins, ligand- receptor based binding, including T-cell receptor antigenic peptide interactions, or major histocompatibility complex (MHC) - antigenic peptide based interactions.
- protein epitope tag based technologies selected from the list of interaction partners including but not limited to: antibodies, and any derivatives, variants or fragments thereof, such as nanobodies, or single-chain fragments (scFv, or scFab), nucleic acid aptamers, and similar proteins, ligand- receptor based binding, including T-cell receptor antigenic peptid
- the candidate interacting entities are provided as protein conjugates comprising a polypeptide sequence (or protein fragment) as interacting portion covalently fused to a nucleic acid sequence which constitutes the labelling portion.
- the invention may also be realized using a phage display library as candidate interacting entity library.
- the interacting portion is provided as a protein presented on the phage coat, and the labelling portion can be a nucleic acid encapsulated within the phage.
- mRNA display is an in vitro selection technique used to obtain from libraries of diverse sequences peptides and proteins that have an affinity for a target ligand/material. The process relies on mRNA-protein fusion molecules, which consist of peptide or protein sequences covalently linked via their C-termini to the 3' end of their own mRNA.
- Yeast display is based on presenting protein variants on the surface of yeast cells. Each cell typically displays only one protein variant of a library, whose identity is encoded in a specihc gene sequence expressed in the corresponding cell (coupling of genotype and phenotype).
- Retroviral display follows the same principles, but the proteins are displayed on the retrovirus membrane and the gene ancoding a particular variant is encapsulated in form of an RNA transfer gene in the corresponding particle.
- the method is performed by using encapsulation into compartments such as any droplet, particle or well, and preferably micro compartments such as into droplets that can be used in a microfluidic system.
- microfluidic droplet refers to an aqueous microcompartment of a certain size that encapsulates an aqueous liquid.
- the size of the microfluidic droplet is usually expressed as the diameter of the droplet when in a spherical shape.
- the diameter is generally between 1 and 500pm, or between 20 and 400 mih, and preferably between 30 and 350 mih, between 40 and 300 mih, between 40 and 250 mih, between 40 and 200 mih or between 40 and too mih (wherein each narrower range is preferred to the foregoing broader ranges and "between” includes the values mentioned).
- the diameter of the microfluidic droplet is between 2 and 20 times the diameter of the largest particle (e.g.
- the diameter of the droplet is defined by both the above absolute and relative parameters.
- the diameter is (i) between 20 and 400 mih, between 30 and 350 mih, between 40 and 300 mih, between 40 and 300 mih, between 40 and 250 mih, between 40 and 200 mih or between 40 and too mih and between 2 and 20 times the diameter of the largest particle (e.g.
- the first particle or a further particle) in the droplet (ii) between 20 and 400 mih, between 30 and 350 mih, between 40 and 300 mih, between 40 and 300 mih, between 40 and 250 mih, between 40 and 200 mih or between 40 and too mih and between 4 and 16 times the diameter of the largest particle (e.g. the first particle or a further particle) in the droplet, or (iii) between 20 and 400 mih, between 30 and 350 mih, between 40 and 300 mih, between 40 and 300 mih, between 40 and 250 mih, between 40 and 200 mih or between 40 and too mih and between 6 and 12 times the diameter of the largest particle (e.g. the first particle or a further particle) in the droplet.
- the size of the microfluidic droplet can also be defined by volume. For example, it is usually less than 1 microlitre (m ⁇ ). Preferably, it is less than 500 nanolitres (nl), less than 250, less than 150, less than too or less than 50 nl or less, such as less than ini, or less than toopl or less. In a preferred embodiment, it is between 0.05 and 150 nl, preferably between 0.05 and 125 nl, between 0.05 and too nl, between 0.05 and 80 nl, or between 0.05 and 4 nl (wherein each narrower range is preferred to the foregoing broader ranges and “between” includes the values mentioned). For screening setups with droplets in the smaller pm range, volumes of less than 1 pi. Microdroplets of the invention for screening purposes have a volume of less than tpl, preferably of 01, or even 0.01 pi.
- Liposomes a practical approach. The practical approach series. Edited by Rickwood, D. & Hames, B. D. Oxford: Oxford University Press) and non-ionic surfactant vesicles (van Hal, D. A., Bouwstra, J. A. & Junginger, H. E. (1996). Nonionic surfactant vesicles containing estradiol for topical application. In Microencapsulation: methods and industrial applications (Benita, S., ed.), pp. 329-347. Marcel Dekker, NewYork.).
- the microcompartments of the present invention are formed from emulsions; heterogeneous systems of two immiscible liquid phases with one of the phases dispersed in the other as droplets of microscopic size
- Emulsions may be produced from any suitable combination of immiscible liquids.
- the emulsion of the present invention has water (containing a particle and other components) as the phase present in the form of droplets and a hydrophobic, immiscible liquid (preferably an oil) as the surrounding matrix in which these droplets are suspended.
- a hydrophobic, immiscible liquid preferably an oil
- Such emulsions are termed 'water- in-oil'.
- the external phase preferably being a hydrophobic oil, generally is inert.
- the emulsion may be stabilized by addition of one or more surface- active agents (surfactants). These surfactants act at the water/oil interface to prevent (or at least delay) separation of the phases.
- oils and many emulsifiers can be used for the generation of water-in-oil emulsions; a recent compilation listed over 16,000 surfactants, many of which are used as emulsifying agents (Ash, M. and Ash, I. (1993) Handbook of industrial surfactants. Gower, Aldershot). Suitable oils are listed below.
- an interaction between two candidate interacting entities may be inducible under certain conditions, including the presence of an interaction inducing small molecular agent (a binding inducing agent).
- an interaction inducing small molecular agent a binding inducing agent
- the invention pertains a method for the identification of at least two interacting entities comprised in two separated libraries of candidate interacting entities, the method comprising the steps of:
- a ratio of entities to compartments which is larger than o and less than l (and preferably is equal to o.i, or larger than o.i and less than l);
- step (d) detecting subsequent to step (c) within the plurality of compartments, which comprise encapsulated entities, a presence of, and preferably an identity of, at least two labelling-portions encapsulated within a single compartment, wherein the presence of two labelling portions within a single compartment is indicative for an interaction between the two candidate interacting entities encapsulated within said compartment.
- purification tag refers to any molecule, or macromolecule (such as peptides, proteins, antibodies and derivatives or fragments thereof, or nucleic acid based tags) suitable for purification or identification of a candidate entity comprising the purification tag.
- the purification tag specifically binds to another moiety with affinity for the purification tag.
- moieties which specifically bind to a purification tag are usually attached to a matrix or a resin, such as agarose beads, used for, for example, column-based purification.
- Moieties which specifically bind to purification tags include antibodies, other proteins (e.g.
- Protein A or Streptavidin Protein A or Streptavidin
- nickel or cobalt ions or resins biotin, amylose, maltose, and cyclodextrin.
- exemplary purification tags include histidine (HIS) tags (such as a hexahistidine peptide), which will bind to metal ions such as nickel or cobalt ions.
- HIS histidine
- Other exemplaiy purification tags are the myc tag, the Strep tag, the Flag tag and the V5 tag.
- the purification tag is selected from the group consisting of a polyhistidine tag, a polyarginine tag, glutathione- S-transferase (GST), maltose binding protein (MBP), influenza virus (HA) tag, thioredoxin, staphylococcal protein A tag, the FLAGTM epitope, and the c-myc epitope.
- GST glutathione- S-transferase
- MBP maltose binding protein
- HA influenza virus
- staphylococcal protein A tag the FLAGTM epitope
- c-myc epitope c-myc epitope.
- the term “purification tag” also includes "epitope tags", i.e. peptide sequences which are specifically recognized by antibodies.
- Exemplary epitope tags include the FLAG tag, which is specifically recognized by a monoclonal anti-FLAG antibody.
- the polypeptide domain fused to the polymerase comprises two or more tags, such as a SUMO tag and a STREP tag.
- the term "purification tag” also includes substantially identical variants of purification tags. "Substantially identical variant” as used herein refers to derivatives or fragments of purification tags which are modified compared to the original purification tag (e.g. via amino acid substitutions, deletions or insertions), but which retain the property of the purification tag of specifically binding to a moiety which specifically recognizes the purification tag.
- Alternative purification tags may include nucleic acid-based tags, such as single stranded nucleic acid sequences that can be bound by their complementary antisense strand.
- each interacting entity of the first entity library comprises a first purification tag not present in the second entity libraiy
- each interacting entity of the second entity library comprises a second purification tag not present in the first entity libraiy
- the purification step (b' ) includes two separate purification steps, wherein a first purification is performed using the first purification tag, and wherein subsequently (and not concomitantly) a second purification is performed using the second purification step.
- the first step is performed in order to reduce the fraction if non-interacting entities comprising the second purification step
- the second purification is performed in order to reduce the fraction of non-interacting entities comprises the first purification tag.
- a “purification” in context of the invention shall therefore comprise a step wherein the entities, or complexes thereof, during purification are brought into contact with a capturing means which specifically bind the purification tag.
- a capturing means which specifically bind the purification tag.
- Such capturing means may be for example a matrix material coupled to the capturing means and thereby allowing affinity-based purification.
- a step of purification allows a use of a less stringent ratio of entities to compartments which is larger than o and less than 1 (preferably less than 0.1).
- a less stringent ratio in preferred embodiments is a ratio of between 0.1 and 1, preferably between 0.2 and, more preferably of between 0.3 and 1, lower than
- the invention pertains to a method for screening for interaction between two entities each of which are comprised in a plurality of entities (library), the method comprising performing the steps of the method of the first aspect.
- the methods of the first and second aspect of the invention are used for screening an interaction that has a therapeutically or diagnostic relevance.
- the methods of the invention maybe used to identify an interaction entity that interacts with a known entity or group of entities, and wherein the interaction entity can be used as a therapeutic.
- the term “comprising” is to be construed as encompassing both “including” and “consisting of’, both meanings being specifically intended, and hence individually disclosed embodiments in accordance with the present invention.
- “and/or” is to be taken as specific disclosure of each of the two specified features or components with or without the other.
- a and/or B is to be taken as specific disclosure of each of (i) A, (ii) B and (iii) A and B, just as if each is set out individually herein.
- the terms “about” and “approximately” denote an interval of accuracy that the person skilled in the art will understand to still ensure the technical effect of the feature in question.
- the term typically indicates deviation from the indicated numerical value by ⁇ 20%, ⁇ 15%, ⁇ 10%, and for example ⁇ 5%.
- the specific such deviation for a numerical value for a given technical effect will depend on the nature of the technical effect.
- a natural or biological technical effect may generally have a larger such deviation than one for a man-made or engineering technical effect.
- the specific such deviation for a numerical value for a given technical effect will depend on the nature of the technical effect.
- a natural or biological technical effect may generally have a larger such deviation than one for a man-made or engineering technical effect.
- Figure 1 shows the general workflow of protein library against library screening. Two libraries of interaction partners that are each physically linked to its self-encoding nucleic acid are incubated together. Subsequently, the interaction partners are encapsulated in water in oil droplets with an occupancy corresponding to less than one interaction partner per droplet volume. Thus, non-interacting entities will most likely end up in separate droplets whereas interacting partners will be encapsulated in the same droplet. During a PCR that is performed in the droplets the DNA strands encoding for the interacting partners are fused together and specific primer sides are introduced at both ends.
- Figure 2 shows an implementation of the workflow shown in Figure 1 using phage display (e.g. an antibody library and a protein target library).
- phage display e.g. an antibody library and a protein target library.
- Figure 3 shows a model system of genetically-encoded interaction partners made of oligonucleotides functionalized with click chemistry moieties (DBCO and Azide). Upon contact and incubation, these functional groups from a covalent bond.
- DBCO and Azide click chemistry moieties
- Figure 4 shows the overview of the workflow and PCR amplification steps of a Proof of Concept test of the invention.
- SPAAC strain-promoted alkyne azide cycloaddition
- a nested PCR was carried out to enrich for the fused fragment (step 5).
- a qPCR with specific primer pairs was done (step 6). Same arrow types represent primers amplifying specifically each individual sequence or fused fragment, specific for every combination of sequences.
- Figure 5 shows the result of the Proof-of-Concept results for the in vitro interaction model system, testing two pairs (Pair A and B) each consisting of two different sequences.
- A Gel image after incubation of Pair A and Pair B (A, B), where either both sequences were modified with DBCO and azide (At, Bi) or only one was modified with DBCO (A2, B2). Only in sample At and Bi an additional band at higher size (At: i.4kb, Bi: l.ikb) can be observed, indicating a successful “click” reaction.
- B Gel image after fusion PCR in droplets.
- Pair A a slightly increased intensity is shown for the fused band (i-5kb) in At compared to A2, while for Pair B, a significant increase in intensity of the fused fragment (i.2kb) is detected in Bi compared to B2.
- Sample A3 and B3 correspond to pre-fused fragments, serving as positive controls.
- Sample C represents the negative control with water.
- C Gel image after nested PCR. Again, a higher band intensity is shown in sample At and Bi for both fused sequences (i-5kb, i.2kb) compared to A2 and B2.
- PCR Ctrl + represents already fused fragments.
- D Table of sample description.
- Samples A1-A3 (At: both sequences modified, A2: one sequence modified, A3: already fused fragment) are referring to Pair A while samples B1-B3 (Bi: both sequences modified, B2: one sequence modified, B3: already fused fragment) indicate samples of Pair B.
- Sample C represents the negative control.
- E qPCR results after nested PCR for Pair A and B, displaying the CT-values of each sample. For Pair A and B, the CT values of sample 1 (At, Bi) are lower than those from sample 2 (A2, B2) confirming the higher concentration and thus successful enrichment of fused fragment compared to the non-interacting sequences.
- Figure 6 shows data published from Kuwabara S, et al. (2021) “Microfluidics sorting enables the isolation of an intact cellular pair complex ofCD8+ T cells and antigen-presenting cells in a cognate antigen recognition-dependent manner.”
- the data shows that high frequency of cellular complex formation is dependent on the specific interaction between T and APC cells.
- the cells were gated using FSC and SSC, following which the cellular complex formation was analyzed using a two-dimensional dot plot.
- CFSE and CMTMR double-positive fractions were derived from the cellular complex between OT-I and ovaAPC. This is a representative plot of three independent experiments.
- Figure 7 shows the result of a pre-purification procedure using HA tagged T7 phage.
- A shows a schematic representation of the experimental setup.
- B shows the result of a quantitative PCRin cT values. Higher cT values indicate lower template concentration in the anaylsed samples samples (first bar indicates qPCR of T7 GFP phages of interaction experiment, second bar indicates qPCR of aGFP nanobody phages of interaction experiment, third bar indicates T7 GFP phages of control experiment, and fourth bar indicates qPCR of JUN of control experiment.
- (C) shows agarose gel of amplification products of nested PCR (3 samples are shown: DD- water control, T7 GFP (Bac) + T7 GFP nanobody (Mam) and T7 GFP (Bac) + T7Jun (Mam).
- Figure 8 shows a pre-purification of interaction partners before applying the method of the invention.
- Example 1 Screening using Protein-Nucleic Acid Conjugates or Phage Display
- Figure 1 shows an implementation of the invention screening for protein-protein interactions using a protein fused to a labelling (or barcoding) nucleic acid.
- two libraries are mixed with each other under conditions that allow for a formation of a binding interaction.
- the mixture is then encapsulated under conditions that provide restriction that not more than one entity or complexed entities is encapsulated within one droplet or compartment on average.
- a fusion PCR is performed within the compartment which subsequently allows for the identification of the presence and identity of interacting proteins.
- Figure 2 shows an implementation using a phage display instead of protein conjugates.
- DBCO Dibenzyl cyclooctyne
- DIBAC Dibenzoazacyclooctyne
- Example 2 Screening interactions of T-cells and antigen presenting cells
- Kuwabara S et al. 2021 used splenocytes from OT-I mice in Ragi knockout background and C57BL/6J WT mice as the antigen-specific and non specific T cells, respectively.
- CD8+ T cells from OT-I transgenic mice recognized OVA-derived peptide SIINFEKL (OVA257-264) bound to H-2Kb of the MHC class I molecule.
- OVA-derived peptide SIINFEKL OVA-derived peptide SIINFEKL (OVA257-264) bound to H-2Kb of the MHC class I molecule.
- Kuwabara S et al. 2021 used the previously established H-2Kb-expressing BW5147 cell line (H2Kb-BW5i47).
- Kuwabara S et al.2021 used both OVA- and H-2Kb-expressing BW5147 cells, which were generated as described in the method section (see Methods of Kuwabara S et al. 2021, incorporated herein by reference). To differentiate these cells, OVA-H2Kb-BW5i47 (ovaAPC), H2Kb-BW5i47 (nullAPC), OT-I, and C57BL/6 (WT) splenocytes were stained with the fluorescent dyes CMTMR, CMAC, CFSE, and Far Red, respectively.
- the screens may be conducted using either genetically modified antigen- presenting cells (in which the antigen is encoded in a known genetic content, e.g. using recombinant expression vectors with specific, known primer binding sites, or alternatively cells expressing peptide-MHC-I fusion proteins in which the presented antigenic peptide is encoded within the presenting cell directly).
- the second cell type is labelled with hash tag antibodies (antibodies binding common epitopes expressed on pretty much any cell and having a specific oligonucleotide barcode and therefore also known primer binding sites for the in-droplet fusion PCR).
- hash tag antibodies antibodies binding common epitopes expressed on pretty much any cell and having a specific oligonucleotide barcode and therefore also known primer binding sites for the in-droplet fusion PCR.
- step 2. After step 2.) and additional encapsulation into droplets at a density of less than 1 phage particle per droplet.
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